United States · FDA National Drug Code directory

Chlorthalidone

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
68382-970_1db5deb3-2699-4c73-a11e-1e4aa12e97fb
Product NDC
68382-970
Form
TABLET
Composition / generic term
Chlorthalidone
Labeler
Zydus Pharmaceuticals USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190515
Source listing expiry
20261231

Source-listed ingredients

  • CHLORTHALIDONE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (68382-970-01) · 68382-970-01
  • 1000 TABLET in 1 BOTTLE (68382-970-10) · 68382-970-10

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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